Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/30—Inkjet printing inks
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/30—Inkjet printing inks
  • C09D11/36—Inkjet printing inks based on non-aqueous solvents
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/05—Alcohols; Metal alcoholates
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/05—Alcohols; Metal alcoholates
  • C08K5/053—Polyhydroxylic alcohols
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/10—Esters; Ether-esters
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/30—Inkjet printing inks
  • C09D11/38—Inkjet printing inks characterised by non-macromolecular additives other than solvents, pigments or dyes

Definitions

• This invention relates to ink jet printer inks, and in particular to such inks comprising a dispersion of a solid colorant in a diluent.
• ink jet printing a fluid ink is forced under pressure, and sometimes at elevated temperature, through a very small nozzle in a printing head.
• a printer known as a "continuous" printer
• ink droplets which are produced continuously are passed through a charging area where individual droplets receive an electrical charge in response to a signal and are directed towards a substrate to be printed.
• the droplets then pass through an electrical field causing them to be deflected by an amount which is dependent on the intensity of the charge and the field.
• Droplets not required to form print on the substrate are directed to a by-pass gutter.
• Inks for use in such printers need to be conductive.
• Drop-on-demand printers can use an electrostatically accelerated ink jet or droplet sequences ejected by pressure impulse actuation.
• each drop of ink is individually ejected from a nozzle by means of pressure pulses induced e.g. by use of a piezo-electric actuator acting on the ink in the channel supplying the nozzle or by generation of a vapour bubble in response to a thermal pulse.
• an ink in the form of a dispersion For an ink in the form of a dispersion to be suitable for use in modern ink jet printers, especially DOD printers, it must meet a number of essential criteria. It must be stable so that phase separation or sedimentation does not occur while the ink is in store or is in the head of the printer; it must have a sufficiently low viscosity that the energy requirements for firing it from a print head are acceptable; it must be capable of being fired from the printhead consistently in the form of single droplets of uniform size and it must dry quickly on the substrate to produce a printed dot of acceptable colour density and a well-defined regular outline. To meet these criteria requires the ink to have a viscosity, surface tension and vaporisation rate within certain well defined limits.
• RMV receding meniscus velocity
• Dispersion inks tend to fall into two groups, those wherein the diluent is aqueous and those wherein it is essentially non-aqueous.
• Aqueous inks are essentially odourless but have certain shortcomings; in particular their drying rate is not as fast as most non-aqueous inks and the print tends not to be water fast.
• Non-aqueous inks are generally quicker drying and give water-fast print; however, the print from non-aqueous ink compositions developed hitherto has tended to exhibit an odour which is considered unpleasant by some users.
• Bohlin CS Rheometer with a CP 4/40 measuring system; preferably no greater than 15 mPa.s, more preferably no greater than 12 mPa.s; a surface tension in the range 22 to 36 rriN.m at 25°C, more preferably 24 to 32; a boiling point greater than 200°C; an RMV of at least 1.0 mm. sec "1 , measured as described in 097/15633, more preferably at least 10 mm.
• 091/15425 describes carbon blacks treated with a treating agent comprising at least one compound containing at least one long chain alkenyl or alkyl group and at least one amine group and news ink compositions containing the treated blacks.
• the treated blacks contain 0.25-20% preferably 0.5-8% of treating agent and to form the inks these treated blacks are dispersed in oils having significant aromatic contents (8.7% and above).
• O95/01404 describes an ink jet ink comprising a liquid having an electrical resistance of at least 10 9 ohm cm, insoluble marking particles and a particle charging agent .
• the ink is designed for use in the type of inkjet printer described in 093/11866. This is a printer having a triangular shaped plate over which the ink flows continually. A charge is applied to the ink to charge the pigment particles which are electrostatically ejected onto the printing media, the majority of the solvent remains on the plate.
• the printer has no nozzle plate and as the ink flows continually over the plate the dispersant requirements of the ink are less stringent than those required in conventional inkjet printing.
• Succinimides are amongst the many classes of compound suggested as particle charging agents but there is no suggestion that succinimides may act as dispersants for the particles.
• an ink jet printer ink composition comprising a dispersion of particulate colorant in a diluent and containing a dispersing agent for the colorant characterised in that the diluent comprises more than 50% by volume of white oil and the composition includes at least one dispersing agent comprising at least one compound having both a long chain aliphatic group and at least one at, ⁇ -dicarboxylic acid moiety, said at least one dispersing agent being present in an amount of at least 20% by weight of the colorant.
• the white oils suitable for use in the invention will contain less than 5% aromatics by weight.
• the white oil is free or substantially free of aromatic components; that is to say it contains not more than 1% aromatics.
• Technical grade white oils are suitable and medicinal and food-grade white oils are preferred.
• the diluent may contain at least one other liquid component in addition to the white oil provided the white oil forms the major component of the diluent by volume and the diluent remains single phase.
• water, if present must be in an amount which is miscible with or soluble in the other component or components of the diluent.
• examples of other components that may be included in admixture with the white oil are other organic liquids provided that they do not interfere with colour, odour and/or stability.
• Liquid fatty acid esters form a preferred class of such liquids.
• the amount of fatty acid ester that may be used will depend upon its nature and properties, eg. volatility, and upon the choice of other components in the formulation but amounts of up to 20% by volume have generally been found acceptable. Even higher amounts may be found useful in some formulations.
• Suitable colorants include, in particular, carbon black and those colorants characterised as pigment dyes in The Colour Index.
• carbon blacks examples include, but are not limited to Regal 250R, Special Black 550, Special Black FW200, Special Black 4, Mogul L, Printex U and Elftex 125.
• Suitable pigments include those within the ranges having the following CI classifications:
• specific pigments include IRGALITE BLUE GLVO, MONASTRAL BLUE FGX, IRGALITE BLUE GLSM, IRGALITE BLUE GLNF, HELIOGEN BLUE L7101F, LUTETIA CYANINE ENJ, HELIOGEN BLUE L6700F, MONASTRAL GREEN GNX-C, MONASTRAL GBX, MONASTRAL GLX, MONASTRAL 6Y, IRGAZIN DPP ORANGE RA, NOVAPERM ORANGE H5G70, NOVPERM ORANGE HL, MONOLITE ORANGE 2R, NOVAPERM RED HFG, HOSTAPERM ORANGE HGL, PALIOGEN ORANGE L2640, SICOFAST ORANGE 2953, IRGAZIN ORANGE 3GL, CHROMOPTHAL ORANGE GP, HOSTAPERM ORANGE GR, PV CARMINE HF4C,
• the colorants are chosen to give the widest range of colours and tones in a hexachrome system.
• the amount of colorant to be employed will depend upon the choice of colorant and the intensity of colour required in the print derived from the ink but will normally be in the range of from 2 to 20 by weight of the ink composition, more preferably from 4 to 15 by weight .
• the dispersant systems employed hitherto for stabilising dispersions of colorants in essentially non-aqueous diluents tend not to be suitable for use in the inks of the present invention because inks containing them tend to have an unacceptable odour.
• this problem may be overcome by using as the dispersant at least one compound containing a long chain aliphatic group and an c-, ⁇ -dicarboxylic acid moiety.
• a long chain aliphatic group is meant in this context an alkyl or alkenyl group having at least 36 carbon atoms in a chain.
• the alkenyl group may contain one or more than one unsaturated carbon- carbon group.
• the group may comprise a polymer or oligomer of an olefin or mixture of olefins, eg. polyisobutene, polybutadiene or ethylene/propylene copolymer.
• the preferred chain length appears to depend upon the nature of the polyolefin.
• polyisobutene the molecular weight is preferably in the range 700 to 5000.
• ethylene/ propylene copolymers however, higher molecular weights may be preferred.
• an c, ⁇ -dicarboxylic acid moiety is meant the free acid or a derivative thereof such as a mono or diester, mono or diamide, anhydride or imide.
• the moities are cyclic eg. as in dicarboxylic acid anhydride or imide, eg. succinic anhydride and succinimides.
• the moiety may be attached directly to the long chain aliphatic group or indirectly via an intermediate atom or group.
• Compounds containing these moities may be obtained, for example, by grafting an ⁇ , ⁇ - ethylenically unsaturated dicarboxylic acid or derivative thereof, eg. maleic anhydride, on to an olefin polymer or copolymer of the desired chain length.
• the compound is selected from long chain alkyl and alkenyl imides such as polyalkenyl succinimides.
• alkenyl imides such as polyalkenyl succinimides.
• Such compounds are obtainable, for example, by grafting an a, ⁇ -ethylenically unsaturated dicarboxylic acid anhydride, typically maleic anhydride, on to a polyolefin, e.g. polyisobutylene or an ethylene/propylene
• the , ⁇ -dicarboxylic acid moiety is an ester, eg. a succinic acid ester.
• the ester is derived from a polyhydric alcohol, eg. dihydric alcohols such as ethylene glycol and propylene glycol, and alcohols having more than three hydroxyl groups, eg. pentaerythritol .
• An example of a suitable material is SAP 210 marketed by Shell.
• anhydride eg. as in succinic anhydride.
• Such compounds are obtainable, for example, by grafting an c-, ⁇ -ethylenically unsaturated dicarboxylic acid anhydride, eg. maleic anhydride, onto a polyolefin, eg. polyisobutylene, polybutadiene, or ethylene propylene copolymer.
• the grafted product may contain one, or more than one, anhydride group attached to the polyolefin backbone.
• An example of a suitable compound is Lithene N4- 5000-3.5MA available from Revertex Chemicals.
• One or more of the compounds having both a long chain aliphatic group and at least one , ⁇ -dicarboxylic acid moiety may be used as the dispersant and in one preferred embodiment, which is particularly advantageous if the colorant includes a component having a basic reaction, eg. as in the case of many black and cyan pigments, the dispersant may comprise at least one imide and at least one anhydride since this may result in enhancement of the stability of the ink composition.
• At least one of the above-defined dispersant compounds also includes boron since its presence appears to improve one or both of stability and the RMV of the ink.
• suitable materials are Paranox 106 and Paranox 1273 from Exxon. The use of boron-containing materials is
• the colorant is a pigment having a basic reaction, eg. as in many black and cyan pigments .
• the amount of dispersant required will depend on the particular dispersant employed and choice of colorant. However, contrary to what might be expected from the article by Pugh et al , referred to above, below 20% of dispersant based on the weight of colorant, it is difficult or impossible to obtain stable dispersions with the formulations of the present invention.
• the dispersant is employed in an amount of 20 to 150% by weight of the colorant, more preferably 40 to 100%.
• the stability of the ink composition of the invention is in many cases dependent upon the nature of the colorant and it has been found that stability may be increased in many of
• composition is still stable in the sense of exhibiting a viscosity rise of no greater than 50% and no clear indication of phase separation in the test defined above, after at least 12 weeks at 70°C.
• dispersant (s) and colorant in addition to the diluent, dispersant (s) and colorant, other components conventionally included in ink jet ink dispersion compositions, eg. dispersant synergists and viscosity modifiers, may be included in the compositions of the present invention.
• dispersant synergists examples are those marketed by Zeneca Colours under the trade name Solsperse.
• viscosity modifiers are Indopol L-100, a polyisobutylene available from Amoco and long chain alkyl alcohols such as Novol , an oleyl alcohol available from Croda.
• a black ink was prepared having the following composition Mogul L 11 parts OLOA 1200 4.4 parts Lytol 84.6 parts
• OLOA is a long chain alkyl succinimide dispersant available from Chevron.
• Lytol is a medical grade white oil available from Witco.
• the formulation was stable for at least 12 weeks at 70°C and had an RMV of 9.
• Estisol 312 is a mixture of saturated coconut fatty acid esters available from Schurmann Ltd of Barnet, England.
• An ink was prepared having the following composition (parts expressed as by weight) .
• Regal Black 250R is a carbon black with a basic reaction, available from Cabot Corporation.
• Lithene N4-5000-3.5MA is a liquid polybutadiene-graft- maleic anhydride available from Revertex Chemicals.
• the product was still stable after 6 weeks at 70 °C.
• An ink was prepared with the following composition (parts expressed as by weight)
• Solsperse 5000 is a substituted ammonium phthalocyanine- type dispersant synergist available from Zeneca Colours.
• the ink showed no significant change in viscosity after 6
• An ink was prepared having the following formulation:
• Paranox 106 is a boronated long chain alkyl or alkenyl succinimide available from Exxon.
• the properties of the ink were as follows:
• a black ink was prepared having the following composition:
• SAP 210 is available from Shell. Klearol is a white oil available from Witco.
• the formulation which had a viscosity at 25°C of about 11, was stable for at least 6 weeks at 70°C.
• Paranox 106 is a boronated polyisobutylene succinimide available from Exxon.
• Paranox 105 and Paranox 1273 are polyisobutylene succinimide dispersants available from Exxon.
• Lubrizol 2153 and Lubrizol 2155 are polyisobutylene succinimide dispersants available from Lubrizol.
• SAP 210 is a long chain aliphatic-substituted succinic ester of a polyhydric alcohol available from Shell.
• SAP 285 is a chlorinated polyisobutylene bis succinimide dispersant available from Shell.
• Solsperse 5000 and Solsperse 22000 are dispersant synergists available from Zeneca Colours.
• Uravar FN5 is an alkyl substituted novolak marketed by DSM of Netherlands.
• Novol is an oleyl alcohol marketed by Croda.
• Indopol L-100 is a polyisobutylene viscosity modifier available from Amoco.
• An ink according to the invention was formed having the following formulation

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Wood Science & Technology (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Inks, Pencil-Leads, Or Crayons (AREA)
• Ink Jet (AREA)

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• 1998
  • 1998-02-02 GB GBGB9802210.6A patent/GB9802210D0/en not_active Ceased
• 1999
  • 1999-02-02 AU AU24334/99A patent/AU2433499A/en not_active Abandoned
  • 1999-02-02 WO PCT/GB1999/000341 patent/WO1999038925A1/en active IP Right Grant
  • 1999-02-02 EP EP99903815A patent/EP1053286B1/de not_active Expired - Lifetime
  • 1999-02-02 DE DE69930924T patent/DE69930924T2/de not_active Expired - Fee Related
  • 1999-02-02 JP JP2000529388A patent/JP3837019B2/ja not_active Expired - Fee Related
  • 1999-02-02 CA CA002317516A patent/CA2317516A1/en not_active Abandoned
  • 1999-02-02 CN CNB998026042A patent/CN1175064C/zh not_active Expired - Fee Related
  • 1999-02-02 KR KR1020007008423A patent/KR20010040555A/ko not_active Application Discontinuation
• 2000
  • 2000-07-13 US US09/615,238 patent/US6476096B1/en not_active Expired - Fee Related

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